Weill Institute of Cell and Molecular Biology, Cornell University, Ithaca, NY, USA; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.
Weill Institute of Cell and Molecular Biology, Cornell University, Ithaca, NY, USA; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.
Trends Cell Biol. 2021 Apr;31(4):269-283. doi: 10.1016/j.tcb.2020.11.011. Epub 2021 Jan 4.
Protein quality control (PQC) machineries play a critical role in selective identification and removal of mistargeted, misfolded, and aberrant proteins. This task is extremely complicated due to the enormous diversity of the proteome. It also requires nuanced and careful differentiation between 'normal' and 'folding intermediates' from 'abnormal' and 'misfolded' protein states. Multiple genetic and proteomic approaches have started to delineate the molecular underpinnings of how these machineries recognize their target and how their activity is regulated. In this review, we summarize our understanding of the various E3 ubiquitin ligases and associated machinery that mediate PQC in the endo-lysosome system in yeast and humans, how they are regulated, and mechanisms of target selection, with the intent of guiding future research in this area.
蛋白质质量控制(PQC)机制在选择性识别和去除靶向错误、错误折叠和异常蛋白质方面发挥着关键作用。由于蛋白质组的巨大多样性,这项任务极其复杂。它还需要在“正常”和“折叠中间体”与“异常”和“错误折叠”蛋白质状态之间进行细微而仔细的区分。多种遗传和蛋白质组学方法已开始阐明这些机制如何识别其靶标以及如何调节其活性的分子基础。在这篇综述中,我们总结了我们对介导酵母和人类内体溶酶体系统 PQC 的各种 E3 泛素连接酶和相关机制的理解,包括它们的调节方式以及靶标选择机制,旨在为该领域的未来研究提供指导。